Canonical Allele Identifier: CA2173753220

Gene: PATL2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711264G= , CM000677.2:g.44711264G=	GRCh38
NC_000015.9:g.45003462G= , CM000677.1:g.45003462G=	GRCh37
NC_000015.8:g.42790754G=	NCBI36
NG_012920.1:g.4778G=
NG_012920.2:g.4788G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682850.1:c.-498C= MANE Select	ENSP00000508024.1:n.-498C=
ENST00000558573.1:n.53C=
XM_011521338.1:c.-498C=	XP_011519640.1:n.-498C=
XM_011521339.1:c.-379C=	XP_011519641.1:n.-379C=
XM_011521340.1:c.-320C=	XP_011519642.1:n.-320C=
XM_011521343.1:c.-582C=	XP_011519645.1:n.-582C=
XM_011521345.1:c.-553C=	XP_011519647.1:n.-553C=
XM_011521338.3:c.-498C=	XP_011519640.1:n.-498C=
XM_011521339.3:c.-379C=	XP_011519641.1:n.-379C=
XM_011521340.3:c.-320C=	XP_011519642.1:n.-320C=
XM_011521343.3:c.-582C=	XP_011519645.1:n.-582C=
XM_011521345.3:c.-553C=	XP_011519647.1:n.-553C=
NM_001387260.1:c.-76+68C=	NP_001374189.1:n.-76+68C=
NM_001387261.1:c.-320C=	NP_001374190.1:n.-320C=
NM_001387262.1:c.-588C=	NP_001374191.1:n.-588C=
NM_001387263.1:c.-498C= MANE Select	NP_001374192.1:n.-498C=